CA2760778A1 - Composes heteroaryle en tant qu'inhibiteurs des pikk - Google Patents
Composes heteroaryle en tant qu'inhibiteurs des pikk Download PDFInfo
- Publication number
- CA2760778A1 CA2760778A1 CA2760778A CA2760778A CA2760778A1 CA 2760778 A1 CA2760778 A1 CA 2760778A1 CA 2760778 A CA2760778 A CA 2760778A CA 2760778 A CA2760778 A CA 2760778A CA 2760778 A1 CA2760778 A1 CA 2760778A1
- Authority
- CA
- Canada
- Prior art keywords
- pyrazol
- methyl
- amino
- alkylene
- imidazo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17782509P | 2009-05-13 | 2009-05-13 | |
US61/177,825 | 2009-05-13 | ||
PCT/US2010/034596 WO2010132598A1 (fr) | 2009-05-13 | 2010-05-12 | Composés hétéroaryle en tant qu'inhibiteurs des pikk |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2760778A1 true CA2760778A1 (fr) | 2010-11-18 |
Family
ID=42470855
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2760778A Abandoned CA2760778A1 (fr) | 2009-05-13 | 2010-05-12 | Composes heteroaryle en tant qu'inhibiteurs des pikk |
Country Status (7)
Country | Link |
---|---|
US (1) | US20120190666A1 (fr) |
EP (1) | EP2430013B1 (fr) |
JP (1) | JP2012526836A (fr) |
AU (1) | AU2010249040B2 (fr) |
CA (1) | CA2760778A1 (fr) |
MX (1) | MX2011012037A (fr) |
WO (1) | WO2010132598A1 (fr) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5581219B2 (ja) | 2008-01-25 | 2014-08-27 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | チオフェンおよびホスファチジルイノシトール3−キナーゼ(pi3k)阻害薬としてのその使用 |
WO2009155121A2 (fr) | 2008-05-30 | 2009-12-23 | Amgen Inc. | Inhibiteurs de la pi3 kinase |
US8796314B2 (en) | 2009-01-30 | 2014-08-05 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
US9139589B2 (en) | 2009-01-30 | 2015-09-22 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
WO2012021611A1 (fr) | 2010-08-11 | 2012-02-16 | Millennium Pharmaceuticals, Inc. | Hétéroaryles et utilisations de ceux-ci |
US8859768B2 (en) | 2010-08-11 | 2014-10-14 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
WO2012021696A1 (fr) | 2010-08-11 | 2012-02-16 | Millennium Pharmaceuticals, Inc. | Hétéroaryles et leurs utilisations |
CN103237450A (zh) | 2010-10-13 | 2013-08-07 | 米伦纽姆医药公司 | 杂芳基化合物和其用途 |
CA2824197C (fr) * | 2011-01-10 | 2020-02-25 | Michael Martin | Procedes de preparation d'isoquinolinones et de formes solides d'isoquinolinones |
JP5808826B2 (ja) * | 2011-02-23 | 2015-11-10 | インテリカイン, エルエルシー | 複素環化合物およびその使用 |
AU2012316055B2 (en) | 2011-09-27 | 2016-05-12 | Amgen Inc. | Heterocyclic compounds as MDM2 inhibitors for the treatment of cancer |
TW201331194A (zh) * | 2011-12-23 | 2013-08-01 | Millennium Pharm Inc | 雜芳基化合物及其用途 |
ES2668279T3 (es) * | 2012-03-15 | 2018-05-17 | Signal Pharmaceuticals, Llc | Tratamiento del cáncer con inhibidores de la cinasa TOR |
BR112015000675B1 (pt) * | 2012-07-13 | 2022-07-12 | UCB Biopharma SRL | Derivados de imidazopiridina como moduladores da atividade de tnf |
CA2901696C (fr) | 2013-02-19 | 2021-04-13 | Amgen Inc. | Cis-morpholinone et autres composes servant d'inhibiteurs de mdm2 pour le traitement du cancer |
EP2970237B1 (fr) | 2013-03-14 | 2017-09-27 | Amgen Inc. | Composés morpholinone d'acide hétéroaryle utilisés comme inhibiteurs de mdm2 pour le traitement du cancer |
CA2907912A1 (fr) * | 2013-05-01 | 2014-11-06 | F. Hoffmann-La Roche Ag | Pyrimidines a substitution heterocycloalkyle liees a c et leurs utilisations |
JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
HUE059351T2 (hu) | 2013-11-11 | 2022-11-28 | Amgen Inc | MDM2 inhibitort és egy vagy több további gyógyszerhatóanyagot tartalmazó kombinációs terápia rákbetegségek kezelésére |
DK3157916T3 (en) | 2014-06-19 | 2019-03-18 | Ariad Pharma Inc | HETEROARYL COMPOUNDS FOR CHINESE INHIBITION |
WO2018013430A2 (fr) | 2016-07-12 | 2018-01-18 | Arisan Therapeutics Inc. | Composés hétérocycliques pour le traitement d'une infection à arenavirus |
TW201813963A (zh) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
TW201825465A (zh) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
TW201815787A (zh) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
JOP20190272A1 (ar) | 2017-05-22 | 2019-11-21 | Amgen Inc | مثبطات kras g12c وطرق لاستخدامها |
EP4141005B1 (fr) | 2017-09-08 | 2024-04-03 | Amgen Inc. | Inhibiteurs de kras g12c et leurs procédés d'utilisation |
AU2019262589B2 (en) | 2018-05-04 | 2022-07-07 | Amgen Inc. | KRAS G12C inhibitors and methods of using the same |
JP2021523208A (ja) | 2018-05-14 | 2021-09-02 | アリアド ファーマシューティカルズ, インコーポレイテッド | ピリミジン誘導体の医薬塩及び障害の処置方法 |
CA3100390A1 (fr) | 2018-06-12 | 2020-03-12 | Amgen Inc. | Inhibiteurs de kras g12c regroupant un cycle de piperazine et utilisation dans le traitement du cancer |
JP7377679B2 (ja) | 2018-11-19 | 2023-11-10 | アムジエン・インコーポレーテツド | がん治療のためのkrasg12c阻害剤及び1種以上の薬学的に活性な追加の薬剤を含む併用療法 |
CN111925366B (zh) * | 2019-05-13 | 2024-04-09 | 广东阿格蕾雅光电材料有限公司 | 一种咪唑并氮杂环化合物及其应用 |
EP3738593A1 (fr) | 2019-05-14 | 2020-11-18 | Amgen, Inc | Dosage d'inhibiteur de kras pour le traitement de cancers |
CN118834208A (zh) | 2019-05-21 | 2024-10-25 | 美国安进公司 | 固态形式 |
KR20220041133A (ko) * | 2019-07-24 | 2022-03-31 | 메르크 파텐트 게엠베하 | 4-(이미다조[1,2-a]피리딘-3-일)-피리미딘 유도체 |
CN114728962A (zh) | 2019-09-18 | 2022-07-08 | 武田药品工业有限公司 | 血浆激肽释放酶抑制剂及其用途 |
US11370803B2 (en) | 2019-09-18 | 2022-06-28 | Takeda Pharmaceutical Company Limited | Heteroaryl plasma kallikrein inhibitors |
US20240139193A1 (en) | 2019-10-15 | 2024-05-02 | Amgen Inc. | Combination therapy of kras inhibitor and shp2 inhibitor for treatment of cancers |
WO2021098777A1 (fr) * | 2019-11-21 | 2021-05-27 | Beigene, Ltd. | Procédés de traitement du cancer utilisant des anticorps anti-ox40 en combinaison avec des inhibiteurs de pi3 kinase delta |
WO2021126816A1 (fr) | 2019-12-16 | 2021-06-24 | Amgen Inc. | Schéma posologique d'un inhibiteur du kras g12c |
CN117396473A (zh) * | 2021-03-17 | 2024-01-12 | 武田药品工业株式会社 | 血浆激肽释放酶的咪唑并吡啶基抑制剂 |
WO2023009475A1 (fr) * | 2021-07-26 | 2023-02-02 | President And Fellows Of Harvard College | Inhibiteurs de rock2 et leurs utilisations |
JP2024529453A (ja) * | 2021-07-30 | 2024-08-06 | チルドレンズ ホスピタル メディカル センター | 多環式irak及びflt3阻害化合物並びにその使用 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6514977B1 (en) * | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
NL1010576C2 (nl) * | 1998-11-17 | 2000-05-18 | Skf Eng & Res Centre Bv | Schroefactuator, omvattende een multifunctionele huls, alsmede een klauw. |
CA2620425A1 (fr) * | 2005-08-31 | 2007-03-08 | Bayer Healthcare Llc | Derives d'anilinopyrazole utilises dans le traitement du diabete |
US7750000B2 (en) * | 2005-09-02 | 2010-07-06 | Bayer Schering Pharma Ag | Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments |
DE102005042742A1 (de) * | 2005-09-02 | 2007-03-08 | Schering Ag | Substituierte Imidazo[1,2b]pyridazine als Kinase-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
JP2009535388A (ja) * | 2006-05-03 | 2009-10-01 | アストラゼネカ アクチボラグ | ピラゾール誘導体、及びそのpi3k阻害薬としての使用 |
WO2008042639A1 (fr) * | 2006-10-02 | 2008-04-10 | Irm Llc | Composés et compositions utilisés en tant qu'inhibiteurs de protéine kinase |
AR067326A1 (es) * | 2007-05-11 | 2009-10-07 | Novartis Ag | Imidazopiridinas y pirrolo -pirimidinas sustituidas como inhibidores de cinasa de lipido |
US8367662B2 (en) * | 2007-10-17 | 2013-02-05 | Novartis Ag | Organic compounds |
AU2008343813B2 (en) * | 2007-12-19 | 2012-04-12 | Amgen Inc. | Inhibitors of PI3 kinase |
MX2011008674A (es) * | 2009-02-18 | 2011-11-04 | Amgen Inc | Compuestos de indol/bencimidazol como inhibidores de quinasa mtor. |
-
2010
- 2010-05-12 CA CA2760778A patent/CA2760778A1/fr not_active Abandoned
- 2010-05-12 MX MX2011012037A patent/MX2011012037A/es active IP Right Grant
- 2010-05-12 JP JP2012510985A patent/JP2012526836A/ja not_active Ceased
- 2010-05-12 EP EP10719514.1A patent/EP2430013B1/fr active Active
- 2010-05-12 AU AU2010249040A patent/AU2010249040B2/en not_active Ceased
- 2010-05-12 WO PCT/US2010/034596 patent/WO2010132598A1/fr active Application Filing
- 2010-05-12 US US13/319,683 patent/US20120190666A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20120190666A1 (en) | 2012-07-26 |
AU2010249040B2 (en) | 2013-08-22 |
MX2011012037A (es) | 2012-02-28 |
EP2430013A1 (fr) | 2012-03-21 |
EP2430013B1 (fr) | 2014-10-15 |
AU2010249040A1 (en) | 2011-12-01 |
WO2010132598A1 (fr) | 2010-11-18 |
JP2012526836A (ja) | 2012-11-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |
Effective date: 20160512 |